HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617316Generated: October 31, 2026
Potassium Carbonate → 4-[4-(2,2-Difluoro-cyclopropylmethoxy)-phenyl]-piperidine hydrochloride
https://huagongshe.com/reaction/1617316
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | tert-Butyl 4-(4-hydroxyphenyl)piperidine-1-carboxylate | HCID 19381871 | — |
| Reactant | Sodium chloride; water | HCID 57417360 | — |
| Reactant | Cyclopropanemethanol, 2,2-difluoro-, 1-methanesulfonate | HCID 58198163 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-[4-(2,2-Difluoro-cyclopropylmethoxy)-phenyl]-piperidine hydrochloride | HCID 89647384 | — |
Reaction Steps
4.48 g (19.2 mmol, 80%) Methanesulfonic acid 2,2-difluoro-cyclopropylmethyl ester are added to 5.93 g (19.2 mmol, 90%) 4-(4-hydroxy-phenyl)-piperidine-1-carboxylic acid tert-butyl ester and 5.36 g (38.5 mmol) K2CO3 in 60 mL DMF. Stirring is continued for 12 h at 50° C. under inert gas atmosphere. After that time, brine (50 mL) is added and the mixture is extracted with EtOAc (3×50 mL). The organic layer is separated, washed with brine, dried over sodium sulphate and the solvent is removed by evaporation. The residue is purified by column chromatography (silica gel; gradient PE:EtOAc 20:1→10:1). The residue is taken up in 20 mL DCM and 100 mL 4N HCl in EtOAc are added dropwise at 0° C. The mixture is stirred for 12 h at rt. After that time, the solvent is removed in vacuo to yield the desired product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765959B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-af5bca9b524d4374936ef868da62e6db |
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| Source note | uspto-grants-2014_07 |
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